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Nanoparticulate carbon black in cigarette smoke induces DNA cleavage and Th17-mediated emphysema

Chronic inhalation of cigarette smoke is the major cause of sterile inflammation and pulmonary emphysema. The effect of carbon black (CB), a universal constituent of smoke derived from the incomplete combustion of organic material, in smokers and non-smokers is less known. In this study, we show tha...

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Autores principales: You, Ran, Lu, Wen, Shan, Ming, Berlin, Jacob M, Samuel, Errol LG, Marcano, Daniela C, Sun, Zhengzong, Sikkema, William KA, Yuan, Xiaoyi, Song, Lizhen, Hendrix, Amanda Y, Tour, James M, Corry, David B, Kheradmand, Farrah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4612775/
https://www.ncbi.nlm.nih.gov/pubmed/26437452
http://dx.doi.org/10.7554/eLife.09623
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author You, Ran
Lu, Wen
Shan, Ming
Berlin, Jacob M
Samuel, Errol LG
Marcano, Daniela C
Sun, Zhengzong
Sikkema, William KA
Yuan, Xiaoyi
Song, Lizhen
Hendrix, Amanda Y
Tour, James M
Corry, David B
Kheradmand, Farrah
author_facet You, Ran
Lu, Wen
Shan, Ming
Berlin, Jacob M
Samuel, Errol LG
Marcano, Daniela C
Sun, Zhengzong
Sikkema, William KA
Yuan, Xiaoyi
Song, Lizhen
Hendrix, Amanda Y
Tour, James M
Corry, David B
Kheradmand, Farrah
author_sort You, Ran
collection PubMed
description Chronic inhalation of cigarette smoke is the major cause of sterile inflammation and pulmonary emphysema. The effect of carbon black (CB), a universal constituent of smoke derived from the incomplete combustion of organic material, in smokers and non-smokers is less known. In this study, we show that insoluble nanoparticulate carbon black (nCB) accumulates in human myeloid dendritic cells (mDCs) from emphysematous lung and in CD11c(+) lung antigen presenting cells (APC) of mice exposed to smoke. Likewise, nCB intranasal administration induced emphysema in mouse lungs. Delivered by smoking or intranasally, nCB persisted indefinitely in mouse lung, activated lung APCs, and promoted T helper 17 cell differentiation through double-stranded DNA break (DSB) and ASC-mediated inflammasome assembly in phagocytes. Increasing the polarity or size of CB mitigated many adverse effects. Thus, nCB causes sterile inflammation, DSB, and emphysema and explains adverse health outcomes seen in smokers while implicating the dangers of nCB exposure in non-smokers. DOI: http://dx.doi.org/10.7554/eLife.09623.001
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spelling pubmed-46127752015-10-22 Nanoparticulate carbon black in cigarette smoke induces DNA cleavage and Th17-mediated emphysema You, Ran Lu, Wen Shan, Ming Berlin, Jacob M Samuel, Errol LG Marcano, Daniela C Sun, Zhengzong Sikkema, William KA Yuan, Xiaoyi Song, Lizhen Hendrix, Amanda Y Tour, James M Corry, David B Kheradmand, Farrah eLife Human Biology and Medicine Chronic inhalation of cigarette smoke is the major cause of sterile inflammation and pulmonary emphysema. The effect of carbon black (CB), a universal constituent of smoke derived from the incomplete combustion of organic material, in smokers and non-smokers is less known. In this study, we show that insoluble nanoparticulate carbon black (nCB) accumulates in human myeloid dendritic cells (mDCs) from emphysematous lung and in CD11c(+) lung antigen presenting cells (APC) of mice exposed to smoke. Likewise, nCB intranasal administration induced emphysema in mouse lungs. Delivered by smoking or intranasally, nCB persisted indefinitely in mouse lung, activated lung APCs, and promoted T helper 17 cell differentiation through double-stranded DNA break (DSB) and ASC-mediated inflammasome assembly in phagocytes. Increasing the polarity or size of CB mitigated many adverse effects. Thus, nCB causes sterile inflammation, DSB, and emphysema and explains adverse health outcomes seen in smokers while implicating the dangers of nCB exposure in non-smokers. DOI: http://dx.doi.org/10.7554/eLife.09623.001 eLife Sciences Publications, Ltd 2015-10-05 /pmc/articles/PMC4612775/ /pubmed/26437452 http://dx.doi.org/10.7554/eLife.09623 Text en © 2015, You et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Human Biology and Medicine
You, Ran
Lu, Wen
Shan, Ming
Berlin, Jacob M
Samuel, Errol LG
Marcano, Daniela C
Sun, Zhengzong
Sikkema, William KA
Yuan, Xiaoyi
Song, Lizhen
Hendrix, Amanda Y
Tour, James M
Corry, David B
Kheradmand, Farrah
Nanoparticulate carbon black in cigarette smoke induces DNA cleavage and Th17-mediated emphysema
title Nanoparticulate carbon black in cigarette smoke induces DNA cleavage and Th17-mediated emphysema
title_full Nanoparticulate carbon black in cigarette smoke induces DNA cleavage and Th17-mediated emphysema
title_fullStr Nanoparticulate carbon black in cigarette smoke induces DNA cleavage and Th17-mediated emphysema
title_full_unstemmed Nanoparticulate carbon black in cigarette smoke induces DNA cleavage and Th17-mediated emphysema
title_short Nanoparticulate carbon black in cigarette smoke induces DNA cleavage and Th17-mediated emphysema
title_sort nanoparticulate carbon black in cigarette smoke induces dna cleavage and th17-mediated emphysema
topic Human Biology and Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4612775/
https://www.ncbi.nlm.nih.gov/pubmed/26437452
http://dx.doi.org/10.7554/eLife.09623
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